Faculty Publications
Permanent URI for this communityhttps://idr.nitk.ac.in/handle/123456789/18736
Publications by NITK Faculty
Browse
6 results
Search Results
Item Porous nickel telluride nanostructures as bifunctional electrocatalyst towards hydrogen and oxygen evolution reaction(Elsevier Ltd, 2017) Bhat, K.S.; Barshilia, H.C.; Nagaraja, H.S.Electrochemical water splitting technology has attracted researchers for the development of next generation fuels. Herein, we report the synthesis of nanostructured porous hollow nickel telluride nanosheets and their use as bifunctional electrocatalyst towards hydrogen and oxygen evolution reaction, anticipating an enhanced performance owing to their 2D sheet like morphology, conductivity, porous nature providing larger catalytic surface for water splitting reaction. In this regard, nickel telluride nanostructures were synthesized via an anion-exchange-reaction between pre-synthesized nickel hydroxide hexagonal nanosheets and tellurium ions under hydrothermal conditions. The as-synthesized nanostructures were characterized for structural, morphological and compositional properties using X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy. Nickel telluride modified electrodes were tested as bifunctional electrocatalyst under acidic and alkaline conditions, through linear sweep voltammetry and constant current chronopotentiometry methods. The modified electrodes revealed an onset potential of ?422 mV and 87.4 mV dec?1 Tafel slope towards HER and overpotential of 679 mV and 151 mV dec?1 Tafel slope towards OER. The lower onset potentials are complimented with excellent electrocatalytic stability. © 2017 Hydrogen Energy Publications LLCItem Porous cobalt chalcogenide nanostructures as high performance pseudo-capacitor electrodes(Elsevier Ltd, 2017) Bhat, K.S.; Shenoy, S.; Nagaraja, H.S.; Sridharan, K.Electrochemical supercapacitor is an essential technology that is pivotal for the development of reliable energy storage devices. Herein, we report the fabrication of supercapacitor electrodes using nanostructured porous cobalt chalcogenide (CoTe2 and CoSe2) electrodes, anticipating an enhanced performance owing to their higher contact area with electrolyte and large pore volume enabling shorter diffusion paths for ion exchange. In this regard, we synthesized CoTe2 and CoSe2 nanostructures via an anion-exchange-reaction between pre-synthesized Co(OH)2 hexagonal nanosheets and chalcogen (tellurium and selenium) ions under hydrothermal conditions. Structural, morphological and compositional properties of the as-synthesized materials are examined using X-ray diffraction, Raman spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy. Pseudo-capacitive properties of CoTe2 and CoSe2 nanostructures as working electrodes are studied through cyclic voltammetry and galvanostatic charge-discharge methods using an electrochemical workstation. CoSe2 electrode delivered a specific capacitance of 951 F g?1 at a scan rate of 5 mV s?1, which surprisingly is almost three times higher in comparison to CoTe2 electrode (360 F g?1). Both CoTe2 and CoSe2 electrodes exhibited good capacitance retention capability for 2500 CV cycles. The superior electrochemical performance of the nanoporous CoSe2 electrode indicate their applicability for high-performance energy storage device applications. © 2017 Elsevier LtdItem Effect of isoelectronic tungsten doping on molybdenum selenide nanostructures and their graphene hybrids for supercapacitors(Elsevier Ltd, 2019) Bhat, K.S.; Nagaraja, H.S.Electrochemical supercapacitors are vital for the advancement of energy storage devices. Herein, we report the synthesis of molybdenum selenide (MoSe 2 ), tungsten-doped molybdenum selenide (W–MoSe 2 ) and their graphene (G) composites (W–MoSe 2 /G) via a facile hydrothermal method. Physiochemical properties of the as-synthesized samples are examined using X-ray diffraction, Raman spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, Brunauer–Emmett–Teller measurements, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray spectroscopy measurements. Used as working electrodes for supercapacitors, MoSe 2 nanostructures could deliver the specific capacitance of 106 F g ?1 at 2 mV s ?1 scan rate. Further, doping with tungsten (W) demonstrates the variation of specific capacitances with 2 M % of tungsten as the optimum doping amount, delivering the maximum specific capacitance of 147 F g ?1 . Furthermore, graphene composites of these nanostructures deliver the enhanced specific capacitances of 248 F g ?1 and complimented with excellent capacitance retention capability of 102% for 20000 cycles. © 2019 Elsevier LtdItem Morphology-dependent electrochemical performances of nickel hydroxide nanostructures(Indian Academy of Sciences, 2019) Bhat, K.S.; Nagaraja, H.S.Electrochemical capacitors form part of the developing technologies in the field of alternative energy sources. In the present work, nickel hydroxide (Ni(OH) 2) nanosheets and microflowers are hydrothermally prepared employing different chemical precursors. Structure, morphology and chemical analysis are conducted using powder X-ray diffraction, field emission scanning electron microscopy and energy-dispersive X-ray spectroscopy measurements. Electrochemical performances as supercapacitor electrodes of the synthesized nanostructures are evaluated through cyclic voltammetry and galvanostatic charge–discharge measurements with three-electrode configurations. The results indicated the specific capacitance of 180 and 417Fg-1 at a scan rate of 5mVs-1 for Ni(OH) 2 nanosheets and microflowers, respectively. The higher specific capacitances for Ni(OH) 2 microflowers could be attributed to the higher specific surface area, morphology, electronic conductivity and porosity. Both Ni(OH) 2 nanostructures exhibited good capacitance retention for 1500 cycles. © 2019, Indian Academy of Sciences.Item Two-Dimensional Cadmium Hydroxide Nanosheets for Electrochemical Capacitors Under High Operating Voltage(Springer, 2020) Bhat, K.S.; Huvinahalli, B.R.; Nagaraja, H.S.Abstract: Electrochemical capacitors are deemed to be the most prospective energy storage devices in the field of alternative energy sources. Here, cadmium hydroxide (Cd(OH)2) nanosheets are hydrothermally synthesized and used as electrodes for supercapacitors. Physiochemical properties of the as-synthesized materials are examined using powder x-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy and energy-dispersive x-ray spectroscopy measurements. Electrochemical investigations reveal an excellent operating potential window of 1.5 V, with the specific capacitance of ? 71 F g?1 at a scan rate of 2 mV s?1. In addition, the Cd(OH)2 electrodes are complemented by good cyclic retention for 2000 cycles. Further, the analysis of the type of charge-storage mechanism reveals prominent contributions from the diffusion-controlled processes. Graphic Abstract: [Figure not available: see fulltext.]. © 2019, The Minerals, Metals & Materials Society.Item Electrochemical hydrogen-storage performance of copper sulfide micro-hexagons(Elsevier Ltd, 2021) Bhat, K.S.; Nagaraja, H.S.Electrochemical hydrogen-storage is one of the prominent energy storage systems. In this work, the hydrothermally synthesized copper sulfide (Cu2S) revealed a unique morphology of micro-hexagons as envisioned through scanning electron microscopy measurements. Electrochemical hydrogen storage (EHS) performance was evaluated using various electrochemical techniques, such as cyclic voltammetry, galvanostatic charge-discharge, and impedance spectroscopy measurements. The hydrogen discharge capacity of ~59.32 mAh g?1 was obtained at an applied current density of 1 A g?1. Further, the analysis of the charge-storage mechanism indicates foremost contributions from the redox processes. The prominent hydrogen storage performance is complimented with reasonable cyclic retention for 2500 cycles. © 2020 Hydrogen Energy Publications LLC
